Evidence map›Paper›PMID 41173975›Full record

ArticleScientific reports2025

Whole-genome nanopore sequencing and automatic downstream analysis of respiratory syncytial virus using RSVTyper.

Duyen Bao Le, Inga Tometten, Nadine Lübke, Martha Paluschinski, Anna-Kathrin Schupp, Lutz Ehlkes, Pascal Kreuzer, Nicole Zacharias, Jörg Timm, Alexander Dilthey and 1 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Duyen Bao Le *Institute of Virology , University Hospital Düsseldorf Heinrich Heine University Düsseldorf , Düsseldorf, Germany.
Inga Tometten *Institute of Virology , University Hospital Düsseldorf Heinrich Heine University Düsseldorf , Düsseldorf, Germany.
Nadine LübkeInstitute of Virology , University Hospital Düsseldorf Heinrich Heine University Düsseldorf , Düsseldorf, Germany.
Martha PaluschinskiInstitute of Virology , University Hospital Düsseldorf Heinrich Heine University Düsseldorf , Düsseldorf, Germany.
Anna-Kathrin SchuppInstitute of Virology , University Hospital Düsseldorf Heinrich Heine University Düsseldorf , Düsseldorf, Germany.
Lutz EhlkesDüsseldorf Health Authority (Gesundheitsamt Düsseldorf) , Düsseldorf, Germany.
Pascal KreuzerDüsseldorf Health Authority (Gesundheitsamt Düsseldorf) , Düsseldorf, Germany.
Nicole ZachariasInstitute for Hygiene and Public Health , University Hospital Bonn , Bonn, Germany.
Jörg TimmInstitute of Virology , University Hospital Düsseldorf Heinrich Heine University Düsseldorf , Düsseldorf, Germany.
Alexander Dilthey *Institute of Medical Microbiology and Hospital Hygiene , University Hospital Düsseldorf Heinrich Heine University Düsseldorf , Düsseldorf, Germany.
Andreas Walker *Institute of Virology , University Hospital Düsseldorf Heinrich Heine University Düsseldorf , Düsseldorf, Germany. andreas.walker@med.uni-duesseldorf.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Respiratory syncytial virus (RSV) is a globally circulating virus, causing severe respiratory infections in infants and the elderly. Two RSV vaccines were recently approved, and passive immunization is now recommended in several countries for all newborns, therefore careful surveillance of RSV variants will be important in the future. We therefore develop an integrated whole genome RSV amplification, sequencing and bioinformatics analysis method ("RSVTyper"; https://anaconda.org/bioconda/rsv-typer ) that is suitable for patient samples as well as wastewater. 243 RSV isolates from 2008 to 2025 and wastewater samples from 2023/2024 were amplified in a multiplex tiling PCR with specific primers, generating 39 amplicons ~ 550 bp in length, and sequenced with Oxford Nanopore Technologies. Sequencing reads of patient isolates were analyzed with the RSVTyper pipeline, a tailored analysis pipeline including automatic reference selection, consensus sequence generation and clade assignment via Nextclade. Amplification and sequencing were successful for 213/243 samples. Whole genomes (> 90% coverage) were obtained from 98% of samples with > 10,000 copies/mL, from 3/14 samples with 1,000-10,000 copies/mL, and from none with < 1,000 copies/mL. Average genome-wide mean depth for successfully sequenced samples was 31,800x with an average mean depth of 41,400x in the F gene. Phylogenetic analysis showed seasonal clade and subtype shifting, with a good representation of clade frequencies from patients in wastewater sequences. No variants with known escape mutations from prophylactic monoclonal antibodies were detected. In conclusion, we developed RSVTyper, a cost-effective and scalable RSV sequencing pipeline by integrating sequencing and bioinformatic analysis. It is suitable for both resource-limited settings and high-throughput applications. It will facilitate enhanced RSV surveillance, allowing for further characterization of the RSV genome and rapid detection of potential escape mutations.

Indexed as

Genome, ViralNanopore SequencingRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsWhole Genome SequencingComputational BiologyHigh-Throughput Nucleotide SequencingHumansPhylogeny

Identifiers

PMID41173975
PMCPMC12578865

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.